FDA NDC Directory · JSON-LD · Markdown

zolmiptriptan

NDC 68462-500 · HUMAN PRESCRIPTION DRUG · TABLET, ORALLY DISINTEGRATING

Generic namezolmitriptan
Labeler / ManufacturerGlenmark Pharmaceuticals Inc., USA
Marketing categoryAbbreviated NDA (generic) · App ANDA202560
Dosage form / routeTABLET, ORALLY DISINTEGRATING · ORAL
Active ingredientsZOLMITRIPTAN (5 mg/1)
Marketing started20130514
Package count1

External sources

Source: openFDA. Public-domain (CC0).